Chen Ting, Han Xiang, Wang Zefen, Li Chaoying, Li Mei, Lan Xiongdiao, Ning Yingying, Wang Jingxin, Liu Pengru
Guangxi Key Laboratory for Polysaccharide Materials and Modifications, School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning 530006, China.
Guangxi Autonomous Region Center for Analysis and Test Research, Nanning 530022, China.
Int J Mol Sci. 2025 Mar 28;26(7):3107. doi: 10.3390/ijms26073107.
In this study, PTA&PMA/NiMoO@NF was synthesized on nickel foam through wet chemical etching to promote the kinetics of the oxygen evolution reaction (OER) effectively. OER benefits from two cationic (Ni and Mo) defects and the optimized electronic configuration of PTA&PMA/NiMoO@NF. Thus, it only needs 200 mV to reach the current density of 10 mA cm in 1.0 mol/L of KOH. This value is nearly 100 mV lower than the value needed by pure NiMoO. After being used as an anode for water splitting in an alkaline solution, the as-obtained catalyst can operate at a current density of 10 mA cm for 24 h of good stability. The synthesis strategy adopted in this study can provide an effective, low-cost, simple, and convenient strategy for improving the OER electrocatalytic performance of other transition metal oxides.
在本研究中,通过湿化学蚀刻在泡沫镍上合成了PTA&PMA/NiMoO@NF,以有效促进析氧反应(OER)的动力学。OER受益于两个阳离子(Ni和Mo)缺陷以及PTA&PMA/NiMoO@NF优化的电子构型。因此,在1.0 mol/L的KOH中,仅需200 mV就能达到10 mA cm的电流密度。该值比纯NiMoO所需的值低近100 mV。用作碱性溶液中水电解的阳极后,所制备的催化剂可在10 mA cm的电流密度下运行24 h,稳定性良好。本研究采用的合成策略可为提高其他过渡金属氧化物的OER电催化性能提供一种有效、低成本、简单且便捷的策略。